Lithographic printing plate precursor and method of preparing the same
US-9223216-B2 · Dec 29, 2015 · US
US2019329545A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2019329545-A1 |
| Application number | US-201916409856-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 12, 2019 |
| Priority date | Nov 16, 2016 |
| Publication date | Oct 31, 2019 |
| Grant date | — |
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A planographic printing plate precursor includes: a support; and an image recording layer which includes a radical initiator, a radical polymerizable component, and a radiation absorption compound, and in which the image recording layer shows two or more peaks of a radical generation amount in a radical generation amount-versus-time curve after exposure to image forming radiation, in which the radical initiator includes an electron-donating radical initiator and an electron-accepting radical initiator, and the radiation absorption compound comprises a compound represented by the following Formula 1.
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What is claimed is: 1 . A planographic printing plate precursor, comprising: a support; and an image recording layer which comprises a radical initiator, a radical polymerizable component, and a radiation absorption compound, and wherein the image recording layer shows two or more peaks of a radical generation amount in a radical generation amount-versus-time curve after exposure to image forming radiation, wherein the radical initiator comprises an electron-donating radical initiator and an electron-accepting radical initiator, and wherein the radiation absorption compound comprises a compound represented by the following Formula 1: wherein, in Formula 1, R 1 represents a group capable of cleaving R 1 —X bond due to exposure to image forming radiation, X represents —S— or —NR N —, R N represents a hydrocarbon group, R 2 and R 3 each independently represent a hydrogen atom or an alkyl group, R 2 and R 3 may be linked to each other to form a ring, Ar 1 and Ar 2 each independently represent a group forming a benzene ring or a group forming a naphthalene ring, Y 1 and Y 2 each independently represent an oxygen atom, a sulfur atom, —NR 0 —, or a dialkylmethylene group, R 4 and R 5 each independently represent an alkyl group, R 6 to R 9 each independently represent a hydrogen atom or an alkyl group, R 0 represents a hydrogen atom, an alkyl group, or an aryl group, and Za represents a counter ion that neutralizes the charge. 2 . The planographic printing plate precursor according to claim 1 , wherein X in Formula 1 represents —S—. 3 . The planographic printing plate precursor according to claim 1 , wherein the radiation absorption compound is a decomposition type radiation absorption compound. 4 . The planographic printing plate precursor according to claim 1 , wherein the electron-donating radical initiator comprises a borate compound. 5 . The planographic printing plate precursor according to claim 4 , wherein the borate compound has one or more aryl groups having an electron-withdrawing group. 6 . The planographic printing plate precursor according to claim 1 , wherein electron-accepting radical initiator comprises an iodonium salt. 7 . The planographic printing plate precursor according to claim 6 , wherein the iodonium salt has an electron-donating group as a substituent. 8 . The planographic printing plate precursor according to claim 1 , wherein a peak interval between a peak of the radical generation amount which is initially generated with respect to time after the exposure to the image forming radiation and at least one of peaks of the radical generation amount which are generated subsequent to the initially generated peak, among the peaks of the radical generation amount, is 40 ms or greater. 9 . The planographic printing plate precursor according to claim 1 , wherein a difference between a highest occupied molecular orbital of the electron-donating radical initiator and a highest occupied molecular orbital of the radiation absorption compound is 0.61 eV or greater. 10 . The planographic printing plate precursor according to claim 1 , wherein a difference between a lowest unoccupied molecular orbital of the electron-accepting radical initiator and a lowest unoccupied molecular orbital of the radiation absorption compound is 0.90 eV or less. 11 . The planographic printing plate precursor according to claim 1 , wherein the image recording layer is removable by at least one selected from the group consisting of dampening water and printing ink. 12 . A plate-making method for a planographic printing plate, the method comprising: subjecting the planographic printing plate precursor according to claim 1 to image-wise light exposure; and removing a non-image area of an image recording layer from the exposed planographic printing plate precursor in the presence of a developer having a pH of 2 to 14. 13 . A plate-making method for a planographic printing plate, the method comprising: subjecting the planographic printing plate precursor according to claim 1 to image-wise light exposure; and supplying at least one selected from the group consisting of printing ink and dampening water on a printing press to remove a non-image area of an image recording layer.
with ethylenic or acetylenic bands in the side chains of the photopolymer · CPC title
the binders being polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers · CPC title
Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds (G03F7/075 takes precedence) · CPC title
by ultraviolet or visible light · CPC title
Developable by an alkaline solution · CPC title
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